Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism - Concepedia

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Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism

12

Citations

42

References

2019

Year

Calvin Sjaarda, Shalandra Wood, Amy J. M. McNaughton, S. Paige Taylor, Melissa L. Hudson, Xudong Liu, Andrea Guerin, Muhammad Ayub

Journal of Human Genetics

Genetic DisorderGeneticsFragile X SpectrumPathologyAutismSporadic CaseDisease Gene IdentificationGenomicsMedicineSplicing VariantVariant Interpretation

References

	Year	Citations

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